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Install and launch IGV before selecting data to visualize
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
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Analyze
For hg38
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For hg19
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Link Out
Sequence Read Archive
DBCLS SRA
NCBI SRA
ENA
Antigen: Input control
wikigenes
PDBj
CellType: PBDE
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX150672
GSM935593: USC ChipSeq PBDE Input UCDavis
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Blood
Cell type
PBDE
Tissue
blood
Lineage
mesoderm
Description
peripheral blood-derived erythroblasts
Attributes by original data submitter
Sample
source_name
PBDE
biomaterial_provider
Farnham lab
lab
USC
lab description
Farnham - University of Southern California
datatype
ChipSeq
datatype description
Chromatin IP Sequencing
cell
PBDE
cell organism
human
cell description
peripheral blood-derived erythroblasts
cell lineage
mesoderm
cell sex
M
treatment
None
treatment description
No special treatment or protocol applies
antibody
Input
antibody description
Control signal which may be subtracted from experimental raw signal before peaks are called.
control
UCDavis
control description
Input library was prepared at UC Davis.
control
UCDavis
control description
Input library was prepared at UC Davis.
controlid
wgEncodeEH001778
Sequenced DNA Library
library_name
GSM935593: USC_ChipSeq_PBDE_Input_UCDavis
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
68722722
Reads aligned (%)
91.3
Duplicates removed (%)
8.3
Number of peaks
1428 (qval < 1E-05)
hg19
Number of total reads
68722722
Reads aligned (%)
90.7
Duplicates removed (%)
9.4
Number of peaks
1566 (qval < 1E-05)
Base call quality data from
DBCLS SRA